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VWF anticorps

VWF Reactivité: Humain Hôte: Chèvre Polyclonal unconjugated
N° du produit ABIN286003
  • Antigène Voir toutes VWF Anticorps
    VWF (Von Willebrand Factor (VWF))
    Reactivité
    • 154
    • 37
    • 26
    • 5
    • 5
    • 3
    Humain
    Hôte
    • 89
    • 78
    • 15
    • 7
    Chèvre
    Clonalité
    • 96
    • 90
    • 1
    Polyclonal
    Conjugué
    • 92
    • 20
    • 15
    • 7
    • 4
    • 4
    • 4
    • 4
    • 4
    • 4
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp VWF est non-conjugé
    Application
    Veuillez nous consulter SVP
    Purification
    Purified
    Immunogène
    VWF antibody was raised in goat using human vWF purified from plasma as the immunogen.
    Isotype
    IgG
    Top Product
    Discover our top product VWF Anticorps primaire
  • Indications d'application
    Optimal conditions should be determined byt he investigator.
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    Lot specific
    Buffer
    Supplied in liquid form with 10 mM HEPES, pH 7.4, 150 mM NaCl, 50 % (v/v) glycerol.
    Conseil sur la manipulation
    Avoid repeated freeze/thaw cycles.
    Product will become viscous but will not freeze. Avoid storage in frost-free freezers. Allow product to warm to room temperature and gently mix before use.
    Dilute only prior to immediate use.
    Stock
    -20 °C
    Stockage commentaire
    Store at -10 to -20 °C.
  • Antigène
    VWF (Von Willebrand Factor (VWF))
    Autre désignation
    VWF (VWF Produits)
    Synonymes
    anticorps VWF, anticorps si:ch1073-474e24.1, anticorps F8VWF, anticorps VWD, anticorps 6820430P06Rik, anticorps AI551257, anticorps B130011O06Rik, anticorps C630030D09, anticorps von Willebrand factor, anticorps Von Willebrand factor, anticorps VWF, anticorps vwf, anticorps Vwf
    Sujet
    Von Willebrand factor (vWF) is a blood glycoprotein involved in hemostasis. It is deficient or defective in von Willebrand disease and is involved in a large number of other diseases, including thrombotic thrombocytopenic purpura, Heyde's syndrome, and possibly hemolytic-uremic syndrome.
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